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Multi System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
Multi System FDA UDI
Generic Name
Orthopaedic joint/limb rongeur FDA UDI
Device Name
Lapidus Ronjeur FDA UDI
Model / Reference
P99-150-0019 FDA UDI
Description
Lapidus Ronjeur FDA UDI

Identifiers

Catalog Number
P99-150-0019 FDA UDI
Primary DI / UDI-DI
00889795040855 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Orthopaedic joint/limb rongeur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic joint/limb rongeur

Multi System by Paragon 28 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic joint/limb rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 0a8e0970-512a-4d2b-bc4e-81c1bc5ca10f 34 fields · synced Jun 8, 2026